CA1201381A - Pest-combating agents, their preparation and use - Google Patents

Pest-combating agents, their preparation and use

Info

Publication number: CA1201381A
Authority: CA; Canada
Prior art keywords: composition according; pyrethroid; weight; dichlorvos; arthropodicidal
Prior art date: 1981-08-18
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Expired

Application number

CA000409563A

Other languages

English (en)

French (fr)

Inventor

Wolfgang Berhrenz

Manfred Schutte

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Bayer AG

Original Assignee

Bayer AG

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1981-08-18

Filing date

1982-08-17

Publication date

1986-03-04

1982-08-17 Application filed by Bayer AG filed Critical Bayer AG

1986-03-04 Application granted granted Critical

1986-03-04 Publication of CA1201381A publication Critical patent/CA1201381A/en

Status Expired legal-status Critical Current

Links

239000000203 mixture Substances 0.000 claims abstract description 54
239000007921 spray Substances 0.000 claims abstract description 14
OEBRKCOSUFCWJD-UHFFFAOYSA-N dichlorvos Chemical compound COP(=O)(OC)OC=C(Cl)Cl OEBRKCOSUFCWJD-UHFFFAOYSA-N 0.000 claims abstract description 13
229950001327 dichlorvos Drugs 0.000 claims abstract description 12
239000000443 aerosol Substances 0.000 claims abstract description 10
239000002728 pyrethroid Substances 0.000 claims abstract description 10
ISRUGXGCCGIOQO-UHFFFAOYSA-N Rhoden Chemical compound CNC(=O)OC1=CC=CC=C1OC(C)C ISRUGXGCCGIOQO-UHFFFAOYSA-N 0.000 claims abstract description 9
239000004480 active ingredient Substances 0.000 claims description 17
241000238421 Arthropoda Species 0.000 claims description 10
241000238631 Hexapoda Species 0.000 claims description 10
238000000034 method Methods 0.000 claims description 5
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
229910052801 chlorine Inorganic materials 0.000 claims description 2
229910052731 fluorine Inorganic materials 0.000 claims description 2
125000001153 fluoro group Chemical group F* 0.000 claims description 2
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 1
229910052794 bromium Inorganic materials 0.000 claims 1
239000000460 chlorine Substances 0.000 claims 1
239000011737 fluorine Substances 0.000 claims 1
239000001257 hydrogen Substances 0.000 claims 1
229910052739 hydrogen Inorganic materials 0.000 claims 1
150000001875 compounds Chemical class 0.000 abstract description 22
230000002195 synergetic effect Effects 0.000 abstract description 2
MDIQXIJPQWLFSD-UHFFFAOYSA-N 3-(2,2-dibromoethenyl)-2,2-dimethylcyclopropane-1-carboxylic acid Chemical compound CC1(C)C(C=C(Br)Br)C1C(O)=O MDIQXIJPQWLFSD-UHFFFAOYSA-N 0.000 abstract 1
229960002483 decamethrin Drugs 0.000 abstract 1
OWZREIFADZCYQD-NSHGMRRFSA-N deltamethrin Chemical compound CC1(C)[C@@H](C=C(Br)Br)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 OWZREIFADZCYQD-NSHGMRRFSA-N 0.000 abstract 1
238000009472 formulation Methods 0.000 description 16
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 15
239000003921 oil Substances 0.000 description 13
241000607479 Yersinia pestis Species 0.000 description 11
ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 10
229940126214 compound 3 Drugs 0.000 description 10
239000003350 kerosene Substances 0.000 description 8
229940125782 compound 2 Drugs 0.000 description 7
229940125904 compound 1 Drugs 0.000 description 6
IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 6
239000003380 propellant Substances 0.000 description 6
241000239223 Arachnida Species 0.000 description 5
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 5
-1 aromatic carbonyl compounds Chemical class 0.000 description 5
239000001273 butane Substances 0.000 description 5
239000003795 chemical substances by application Substances 0.000 description 5
230000000694 effects Effects 0.000 description 5
239000000463 material Substances 0.000 description 5
OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 5
239000002304 perfume Substances 0.000 description 5
239000001294 propane Substances 0.000 description 5
239000003381 stabilizer Substances 0.000 description 5
239000008096 xylene Substances 0.000 description 5
VEMKTZHHVJILDY-UXHICEINSA-N bioresmethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-UXHICEINSA-N 0.000 description 4
238000003197 gene knockdown Methods 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
150000002148 esters Chemical class 0.000 description 3
239000004033 plastic Substances 0.000 description 3
229920003023 plastic Polymers 0.000 description 3
239000002904 solvent Substances 0.000 description 3
241001143309 Acanthoscelides obtectus Species 0.000 description 2
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 2
241000255925 Diptera Species 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
241000257303 Hymenoptera Species 0.000 description 2
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
241001465754 Metazoa Species 0.000 description 2
241000257159 Musca domestica Species 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
GQPLMRYTRLFLPF-UHFFFAOYSA-N Nitrous Oxide Chemical compound [O-][N+]#N GQPLMRYTRLFLPF-UHFFFAOYSA-N 0.000 description 2
239000004743 Polypropylene Substances 0.000 description 2
241001481703 Rhipicephalus <genus> Species 0.000 description 2
239000002253 acid Substances 0.000 description 2
150000001298 alcohols Chemical class 0.000 description 2
239000004411 aluminium Substances 0.000 description 2
229910052782 aluminium Inorganic materials 0.000 description 2
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
150000004657 carbamic acid derivatives Chemical class 0.000 description 2
239000011521 glass Substances 0.000 description 2
239000002917 insecticide Substances 0.000 description 2
239000002184 metal Substances 0.000 description 2
229910052751 metal Inorganic materials 0.000 description 2
229920001155 polypropylene Polymers 0.000 description 2
230000001681 protective effect Effects 0.000 description 2
239000005028 tinplate Substances 0.000 description 2
GKASDNZWUGIAMG-UHFFFAOYSA-N triethyl orthoformate Chemical compound CCOC(OCC)OCC GKASDNZWUGIAMG-UHFFFAOYSA-N 0.000 description 2
UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 1
GTJOHISYCKPIMT-UHFFFAOYSA-N 2-methylundecane Chemical compound CCCCCCCCCC(C)C GTJOHISYCKPIMT-UHFFFAOYSA-N 0.000 description 1
HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 1
241000934064 Acarus siro Species 0.000 description 1
241000238818 Acheta domesticus Species 0.000 description 1
241000238679 Amblyomma Species 0.000 description 1
241000411449 Anobium punctatum Species 0.000 description 1
241000256186 Anopheles <genus> Species 0.000 description 1
241001640910 Anthrenus Species 0.000 description 1
241000131286 Attagenus Species 0.000 description 1
241000238662 Blatta orientalis Species 0.000 description 1
241000238657 Blattella germanica Species 0.000 description 1
241000257163 Calliphora vicina Species 0.000 description 1
241001098608 Ceratophyllus Species 0.000 description 1
241001327638 Cimex lectularius Species 0.000 description 1
241000254173 Coleoptera Species 0.000 description 1
241000256054 Culex <genus> Species 0.000 description 1
241001481695 Dermanyssus gallinae Species 0.000 description 1
241001124144 Dermaptera Species 0.000 description 1
241001641895 Dermestes Species 0.000 description 1
241000255601 Drosophila melanogaster Species 0.000 description 1
241000122098 Ephestia kuehniella Species 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
241000371383 Fannia Species 0.000 description 1
241000720914 Forficula auricularia Species 0.000 description 1
241000255896 Galleria mellonella Species 0.000 description 1
241001043186 Gibbium Species 0.000 description 1
241001466007 Heteroptera Species 0.000 description 1
241001480803 Hyalomma Species 0.000 description 1
241000832180 Hylotrupes bajulus Species 0.000 description 1
SGVYKUFIHHTIFL-UHFFFAOYSA-N Isobutylhexyl Natural products CCCCCCCC(C)C SGVYKUFIHHTIFL-UHFFFAOYSA-N 0.000 description 1
241000256602 Isoptera Species 0.000 description 1
241000238681 Ixodes Species 0.000 description 1
241000256686 Lasius <genus> Species 0.000 description 1
241000238866 Latrodectus mactans Species 0.000 description 1
241000255777 Lepidoptera Species 0.000 description 1
241000500881 Lepisma Species 0.000 description 1
241000257162 Lucilia <blowfly> Species 0.000 description 1
241001177134 Lyctus Species 0.000 description 1
241000952627 Monomorium pharaonis Species 0.000 description 1
241000257229 Musca <genus> Species 0.000 description 1
241000257226 Muscidae Species 0.000 description 1
241001385056 Niptus hololeucus Species 0.000 description 1
241000238887 Ornithodoros Species 0.000 description 1
241000238814 Orthoptera Species 0.000 description 1
241000131101 Oryzaephilus surinamensis Species 0.000 description 1
241000238675 Periplaneta americana Species 0.000 description 1
239000004952 Polyamide Substances 0.000 description 1
239000004698 Polyethylene Substances 0.000 description 1
241001105129 Ptinus Species 0.000 description 1
241001509970 Reticulitermes <genus> Species 0.000 description 1
241000722249 Rhodnius prolixus Species 0.000 description 1
241001510236 Rhyparobia maderae Species 0.000 description 1
241000318997 Rhyzopertha dominica Species 0.000 description 1
241000522594 Scorpio maurus Species 0.000 description 1
241000258242 Siphonaptera Species 0.000 description 1
241000254181 Sitophilus Species 0.000 description 1
241001494139 Stomoxys Species 0.000 description 1
241000255626 Tabanus <genus> Species 0.000 description 1
241000254109 Tenebrio molitor Species 0.000 description 1
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 1
241001414833 Triatoma Species 0.000 description 1
241000254086 Tribolium <beetle> Species 0.000 description 1
241000267823 Trogoderma Species 0.000 description 1
241000353223 Xenopsylla cheopis Species 0.000 description 1
241001414985 Zygentoma Species 0.000 description 1
239000000654 additive Substances 0.000 description 1
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
238000000889 atomisation Methods 0.000 description 1
238000009835 boiling Methods 0.000 description 1
239000001569 carbon dioxide Substances 0.000 description 1
229910002092 carbon dioxide Inorganic materials 0.000 description 1
150000001768 cations Chemical class 0.000 description 1
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
125000001309 chloro group Chemical group Cl* 0.000 description 1
238000011161 development Methods 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
230000008030 elimination Effects 0.000 description 1
238000003379 elimination reaction Methods 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
238000005516 engineering process Methods 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
239000007789 gas Substances 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
238000011835 investigation Methods 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
VKPSKYDESGTTFR-UHFFFAOYSA-N isododecane Natural products CC(C)(C)CC(C)CC(C)(C)C VKPSKYDESGTTFR-UHFFFAOYSA-N 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
239000004922 lacquer Substances 0.000 description 1
239000007788 liquid Substances 0.000 description 1
150000002739 metals Chemical class 0.000 description 1
UFEJKYYYVXYMMS-UHFFFAOYSA-N methylcarbamic acid Chemical compound CNC(O)=O UFEJKYYYVXYMMS-UHFFFAOYSA-N 0.000 description 1
239000001272 nitrous oxide Substances 0.000 description 1
125000001117 oleyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
150000002924 oxiranes Chemical class 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
229920002647 polyamide Polymers 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
229920000915 polyvinyl chloride Polymers 0.000 description 1
239000004800 polyvinyl chloride Substances 0.000 description 1
238000012545 processing Methods 0.000 description 1
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
239000003566 sealing material Substances 0.000 description 1
WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 1
239000004299 sodium benzoate Substances 0.000 description 1
235000010234 sodium benzoate Nutrition 0.000 description 1
239000007787 solid Substances 0.000 description 1
238000005507 spraying Methods 0.000 description 1
239000000758 substrate Substances 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
239000011885 synergistic combination Substances 0.000 description 1
238000012360 testing method Methods 0.000 description 1
239000000341 volatile oil Substances 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1

Classifications

- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/10—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
- A01N57/12—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing acyclic or cycloaliphatic radicals
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N53/00—Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof

Landscapes

Life Sciences & Earth Sciences (AREA)
Agronomy & Crop Science (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Coloring (AREA)

CA000409563A 1981-08-18 1982-08-17 Pest-combating agents, their preparation and use Expired CA1201381A (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DE19813132610 DE3132610A1 (de)	1981-08-18	1981-08-18	Schaedlingsbekaempfungsmittel, ihre herstellung und verwendung
DEP3132610.2		1981-08-18

Publications (1)

Publication Number	Publication Date
CA1201381A true CA1201381A (en)	1986-03-04

Family

ID=6139562

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA000409563A Expired CA1201381A (en)	1981-08-18	1982-08-17	Pest-combating agents, their preparation and use

Country Status (20)

Country	Link
US (1)	US4863909A (de)
EP (1)	EP0072515B1 (de)
JP (1)	JPS5839607A (de)
KR (1)	KR900000186B1 (de)
AR (1)	AR247657A1 (de)
AT (1)	ATE21321T1 (de)
AU (1)	AU569463B2 (de)
BR (1)	BR8204795A (de)
CA (1)	CA1201381A (de)
DE (2)	DE3132610A1 (de)
DK (1)	DK156754C (de)
EG (1)	EG15753A (de)
GR (1)	GR76256B (de)
IL (1)	IL66556A (de)
NZ (1)	NZ201597A (de)
OA (1)	OA07187A (de)
PH (1)	PH17901A (de)
PT (1)	PT75399B (de)
TR (1)	TR21808A (de)
ZA (1)	ZA825945B (de)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP2548981B2 (ja) *	1987-03-13	1996-10-30	住友化学工業株式会社	安定な農薬固型製剤
DE4417742A1 (de)	1994-05-20	1995-11-23	Bayer Ag	Nicht-systemische Bekämpfung von Parasiten
CN1047502C (zh) *	1996-03-20	1999-12-22	赵明智	一种含有敌敌畏甲氰菊酯的农药组合物
US6903093B2 (en) *	2000-10-06	2005-06-07	Monsanto Technology Llc	Seed treatment with combinations of pyrethrins/pyrethroids and thiamethoxam
US6838473B2 (en) *	2000-10-06	2005-01-04	Monsanto Technology Llc	Seed treatment with combinations of pyrethrins/pyrethroids and clothiandin
US6660690B2 (en) *	2000-10-06	2003-12-09	Monsanto Technology, L.L.C.	Seed treatment with combinations of insecticides

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2865943A (en) *	1954-05-25	1958-12-23	Bayer Ag	Process of making o, o-dimethyl-o-(beta, beta-dichlorovinyl)-phosphate
NL254339A (de) *	1959-07-31
US2956073A (en) *	1960-04-13	1960-10-11	Shell Oil Co	Insecticidally active esters of phosphorus acids and preparation of the same
JPS4818807B1 (de) *	1969-06-10	1973-06-08
US3891759A (en) *	1970-06-11	1975-06-24	Robert Aries	Stabilized slow release DDUP composition
CY1259A (en) *	1976-12-24	1984-11-23	Wellcome Found	Synergistic parasiticidal compositions
DE2709264C3 (de) *	1977-03-03	1982-01-21	Bayer Ag, 5090 Leverkusen	Substituierte Phenoxybenzyloxycarbonylderivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Insektizide und Akarizide sowie neue Zwischenprodukte
US4357348A (en) *	1978-12-08	1982-11-02	Sumitomo Chemical Company, Limited	Insecticidal and/or acaricidal composition exhibiting low toxicity to mammals and fish
DE2928465A1 (de) *	1979-07-13	1981-01-29	Bayer Ag	Schaedlingsbekaempfungsmittel
DE2932920A1 (de) *	1979-08-14	1981-04-09	Bayer Ag, 5090 Leverkusen	Ektoparasitizide mittel enthaltend substituierte phenoxybenzyloxy-carbonylderivate und carbaminsaeureester, verfahren zu ihrer herstellung und ihre verwendung zur bekaempfung von ektoparasiten
JPS56120607A (en) *	1980-02-26	1981-09-22	Sankyo Co Ltd	Insecticide composition
DE3109476A1 (de) *	1981-03-12	1982-09-23	Bayer Ag, 5090 Leverkusen	Schaedlingsbekaempfungsmittel, ihre herstellung und verwendung

1981
- 1981-08-18 DE DE19813132610 patent/DE3132610A1/de not_active Withdrawn
1982
- 1982-08-09 DE DE8282107170T patent/DE3272569D1/de not_active Expired
- 1982-08-09 AT AT82107170T patent/ATE21321T1/de not_active IP Right Cessation
- 1982-08-09 PT PT75399A patent/PT75399B/pt not_active IP Right Cessation
- 1982-08-09 EP EP82107170A patent/EP0072515B1/de not_active Expired
- 1982-08-12 PH PH27711A patent/PH17901A/en unknown
- 1982-08-13 JP JP57139988A patent/JPS5839607A/ja active Granted
- 1982-08-13 GR GR69040A patent/GR76256B/el unknown
- 1982-08-16 TR TR21808A patent/TR21808A/xx unknown
- 1982-08-16 AU AU87178/82A patent/AU569463B2/en not_active Ceased
- 1982-08-16 IL IL66556A patent/IL66556A/xx not_active IP Right Cessation
- 1982-08-16 NZ NZ201597A patent/NZ201597A/en unknown
- 1982-08-17 OA OA57779A patent/OA07187A/xx unknown
- 1982-08-17 EG EG82500A patent/EG15753A/xx active
- 1982-08-17 BR BR820495A patent/BR8204795A/pt not_active IP Right Cessation
- 1982-08-17 DK DK367982A patent/DK156754C/da not_active IP Right Cessation
- 1982-08-17 ZA ZA825945A patent/ZA825945B/xx unknown
- 1982-08-17 CA CA000409563A patent/CA1201381A/en not_active Expired
- 1982-08-18 AR AR82290333A patent/AR247657A1/es active
- 1982-08-18 KR KR8203708A patent/KR900000186B1/ko active
1985
- 1985-02-13 US US06/701,066 patent/US4863909A/en not_active Expired - Fee Related

Also Published As

Publication number	Publication date
IL66556A0 (en)	1982-12-31
GR76256B (de)	1984-08-04
JPS5839607A (ja)	1983-03-08
EP0072515A2 (de)	1983-02-23
PT75399A (en)	1982-09-01
TR21808A (tr)	1985-07-19
AU569463B2 (en)	1988-02-04
KR840000873A (ko)	1984-03-26
ZA825945B (en)	1983-07-27
DK156754B (da)	1989-10-02
IL66556A (en)	1985-07-31
ATE21321T1 (de)	1986-08-15
EP0072515B1 (de)	1986-08-13
AU8717882A (en)	1983-02-24
DK367982A (da)	1983-02-19
JPH0541601B2 (de)	1993-06-24
KR900000186B1 (ko)	1990-01-23
EG15753A (en)	1986-06-30
OA07187A (fr)	1984-04-30
DK156754C (da)	1990-02-19
NZ201597A (en)	1985-05-31
DE3132610A1 (de)	1983-03-10
PT75399B (en)	1984-12-10
PH17901A (en)	1985-01-25
EP0072515A3 (en)	1983-03-09
US4863909A (en)	1989-09-05
AR247657A1 (es)	1995-03-31
BR8204795A (pt)	1983-08-02
DE3272569D1 (en)	1986-09-18

Legal Events

Date	Code	Title	Description
2003-03-04	MKEX	Expiry

Publication	Publication Date	Title
CA1312876C (en)	1993-01-19	2,3,5,6-tetrafluorobenzyl (+)1r-trans-2,2-dimethyl -3-(2,2-dichlorovinyl)-cyclopropanecarboxylate
CA1201381A (en)	1986-03-04	Pest-combating agents, their preparation and use
JPS59212403A (ja)	1984-12-01	有害生物防除剤
AU627445B2 (en)	1992-08-27	Arthropodicidal compositions
CN1102339C (zh)	2003-03-05	杀虫气雾组合物及制备该组合物的杀虫组合物
CA1169771A (en)	1984-06-26	Pest-combating agents, their preparation and use
SU735150A3 (ru)	1980-05-15	Инсектоакарицидна композици
US4983591A (en)	1991-01-08	Environmentally safe, broad spectrum insecticide
DE3030661A1 (de)	1982-04-01	Hetaryl-propargylether, ihre herstellung und ihre verwendung in schaedlingsbekaempfungsmitteln, diese stoffe enthaltende schaedlingsbekaempfungsmittel, sowie ihre herstellung und verwendung
CS215067B2 (en)	1982-07-30	Insecticide and/or acaricide means and method of making the active substances
EP0477676B1 (de)	1995-01-04	Pyrethroid-Wirkstoffkombinationen enthaltend Benfluthrin und Prallethrin
EP0072516B1 (de)	1986-06-25	Chrommischkomplex-Farbstoffe
Gaines et al.	1950	Toxicity of various sulphur and phosphorus compounds applied as sprays on spider mites and aphids
US3538226A (en)	1970-11-03	Method of destroying plant fungi
Chadwick	1979	The activity of some pyrethroids against Periplaneta americana and Blattella germanica
EP0116889B1 (de)	1986-04-23	Cyclopropylmethyl(en)ether, Verfahren zu ihrer Herstellung und ihre Verwendung in Schädlingsbekämpfungsmitteln
DE2945689A1 (de)	1981-06-04	Neue oxybenztriazolderivate, verfahren zu ihrer herstellung und ihre verwendung als synergisten in schaedlingsbekaempfungsmitteln
Gersdorff et al.	1955	A Comparison of Cyclethrin, Allethrin, Pyrethrins, and Mixtures of Piperonyl Butoxide or Sulf oxide with Them in House Fly Sprays
GB1586653A (en)	1981-03-25	Substituted triazin -2,4-diones and their use as pesticides
US3962457A (en)	1976-06-08	Methods of killing mites using S-β-naphthylmethyl-N,N-dimethylthiolcarbamate
EP0174515A2 (de)	1986-03-19	Phosphorheterocyclen enthaltende Schädlingsbekämpfungsmittel
KR910002219B1 (ko)	1991-04-08	살충제 조성물
EP0044008B1 (de)	1984-12-05	Verwendung von 2-Propargyloxy-benzazolen als Synergisten
DE3026957A1 (de)	1982-02-11	2-propargyloxy-benzazole enthaltende schaedlingsbekaempfungsmittel, ihre herstellung und verwendung
DD210599A5 (de)	1984-06-20	Schaedlingsbekaempfungsmittel